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Crohn's Disease Forum

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Dec 13, 2011
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Okay, so, I guess I'll start out by telling my story. Sorry about the length but it's been a crazy year. I'm 21 years old, always been healthy, don't smoke, drink, or do drugs. In August of this year, I started having horrible cramps and diarrhea. Sometimes there was blood in the stool. I went to the doctor and she prescribed me bentyl for the cramps and told me the diarrhea was probably caused from stress. The bentyl helped for one day then the cramps flared up again. So, I went back to the doctor 4 days later. They did blood and stool tests then put me on flagyl because they thought it was some kind of bacterial infection (even though the tests all came back negative). Later in August, I went into the emergency room because I was so dehydrated. They pumped me full of IV fluids and sent me on my way with instructions to continue the flagyl. September 2nd, I had to go back to the emergency room because nothing was getting better and I continued to have horrible cramps and uncontrollable diarrhea. They gave me IV fluids, more bentyl, more flagyl, and potassium. I was released 5 days later and told to take prednisone along with the rest of my prescription cocktail. To my surprise, I kept getting worse. I started vomiting, couldn't keep anything down (not even water), and started losing weight. About a week later, I was admitted into the hospital again. This time, my GI doctor decided to do a sigmoidoscopy. My dad begged him to do a full colonoscopy but the doc said no because he was afraid my colon might rupture. They finally diagnosed me with Ulcerative Colitis and started me on Asacol, lots and lots of Asacol. I spent another 6 days in the hospital getting pumped full of IV fluids and antibiotics then went on my way. My cramps kept getting worse and worse until I couldn't walk or do anything for myself. I was constantly in pain. My husband had to help me change clothes and realized that my stomach had turned gray. That really scared him so we made another trip to the emergency room. There, they did an Xray to find out that my colon was indeed ruptured. I was CareFlited to the nearest large hospital where they performed emergency surgery to remove 90% of my dead colon. It was actually ruptured in 2 places. I was in septic shock and had 3 different funguses in the abdomen. My surgeon said it was the worst he's ever seen and told my dad and hubby that I probably wouldn't make it. I was put into a medically induced coma for 5 days because I was on Xigris and they said I'd be in too much pain to be awake. The first 2 days after surgery, my heart rate stayed steady at 175-180 because of all the infection. One of my lungs collapsed during surgery so I had a respirator tube down my throat. On top of that, I had 3 pic lines (neck, arm, and pelvis), 3 tubes coming out of my stomach to drain the infection, and a tube going up my nose to keep anything from going into my stomach. My body was swollen to twice my normal body size and I kept running a pretty high fever. I had a freezing blanket on top of me for 48 hours to try and break the fever. I was also handcuffed to the bed so I wouldn't pull out the tube in my throat. I was getting 1 mg of dilotids every 30 minutes. Mind you, this is all what my family has told me because I was completely out of it. My husband won't talk about it anymore because he was pretty sure that he was going to lose me. After 5 days, they finally woke me up and took out all of the tubes except 2 of the pic lines. After a couple more days in the ICU, I was finally transferred into a normal room. I was non-contact (which meant that everyone who came into my room had to wear gloves and a gown so I wouldn't get another infection). I haven't done a final count but I had a team of about 20 doctors. I was told I was the youngest person in the hospital and had the most interesting case. Oh, I forgot to mention that a couple days after surgery, I had a wound vac put into my into my 10 inch incision to suck out all the infection. (A wound vac is when they put a sponge into your incision, then hook it up to a mini vaccuum to suck out all the fluids.) They had to change the sponge every 3-5 days and let me tell you, that was the worst pain I have ever been in. My dad couldn't stand to stay in the room because I would scream and cry. When they took it out, you could see pretty much all of my insides. My husband always stayed in the room to hold my hand through it all but he said it took everything he had to not get sick. I've been told having a wound vac is worse pain than labor. Anyways, I stayed in the hospital for 23 days because my heart rate and white blood cell count kept going up and down. I had an ultrasound done on my heart and found out that the sac around my heart was swollen so I was put on Korig and Lisonopril. I don't remember what this procedure was called but a pulmonologist came in, stuck an ice pick into my back, and drained a liter of fluid from the sac around my lungs. It's called sympathy fluid or something like that. There's so much more that I don't care to remember (5 blood transfusions, being dropped by a physical therapist, etc.) but this is a rundown of the more serious stuff. Oh yeah, I also have an ileostomy and I've lost 56 pounds. I do love being super skinny, haha.
Anyways, here are my questions:
1. Am I ever going to stop losing my hair?! I'm so annoyed by this. Supposedly, it's because of the medication but right now, I'm only taking Asacol and tapering off of Zoloft (I've never been depressed before but 23 days in the hospital can do that to you).
2. Will I be on Asacol forever?
3. Is there anybody out there with about 6 inches of their sigmoid colon left that has had an ileostomy reversal? If so, how'd it go? Do you have normal bowel movement? Is it worth it? The doctors said I may not even be a candidate for a reversal but if I am, it'll at least have to wait a year.
4. Will I ever be able to eat fruits and veggies again? I've tried eating a couple bites here and there, but I always end up throwing up. I miss them so much.
5. Does anybody have any recommendations on how to keep your ileostomy bag from itching under the wafer? I keep it clean and everything and it doesn't leak; I just have really sensitive skin.
6. Do most people have a colonoscopy to diagnose UC? My dad thinks that I should have had one my 2nd visit to the hospital because even if my colon did rupture, I would have been completely cleaned out and already on the operating table.
Sorry about the length again. I'm just so shocked that all this happened in a matter of 3 months. I'd love any feedback :)
 
I'm not sure how to comment on the back story, but damn.

So to the questions that I can answer, unfortunately I can't answer all of them.

2. You might not be on it forever, but there is a chance that you will, it really depends on how well you heal. It's generally a drug for maintaining remission. it acts as a topical agent reducing inflammation and helps t protect the lining of the colon.

4. if all goes well you should be able to eat fruit and veg in some format, over time you should be able to figure out which ones cause you issues.

5. Get some stoma powder it helps greatly, also try a different brand of bag that may help. The companies that make them will send you samples,some are more generous that others.

6. Most people do have a colonoscopy to diagnose, but with that said. The inflammation starts at the base of the colon near the rectum, a full scope is not required to diagnose a person with UC. It is most likely required for Crohn's as the inflammation as not set pattern. But UC it always starts at the bottom and moves up. I've never had a scope done in an operating room, and I've been fully conscious for most of them. Most likely they saw the inflammation and wanted to try and get in under control without the risk of damaging.

quite often unless it is very apparent they diagnose IBD and then sort out which one, the treatment methods are almost identical.

Finally head over to the stoma forum, there is lots of information there.
 
AWESOME! You've actually been tons of help. I'm going to see if I can get some different bags!

Courtney

"Is your bag full or are you just happy to see me?"
 
Courtney,
Glad I could help.
I've also have only ever met awesome Courtneys, I'm friends with two of them, a good one and an evil one.
 
Hello Courtney,
I lost half my hair after being very ill with a severe anaphylactic reaction to flagyl and
ciprofloxacin.It was very upsetting to say the least, together with other skin problems due to the reaction.
The dermatologist told me that the hair cells stopped activity since they thought I was dying and she said that it happens sometimes three months after the event, but that it would probably grow back.
I found a reference to biotin being useful to grow the hair back and take 1mg daily.\Some take 5mg daily but I was afraid to go that far. It is water soluble so the body would expel the excess in urine.
My hair has now grown back very well and has a good texture again.It has taken about 4 months to get it back though.I am glad I took the biotin, and also I use Jason biotin
shampoo regularly.
Sorry you have had such a terrible time and hope you continue on the path of wellness.
Hugs and best wishes
Trysha
 
You sound like such a fighter; kudos to you! Keep searching and asking questions and I am sure you will be on your way to recovery! Never give up hope; no matter what the docs say.. You are already proof of that! I was told I would never get rid of my Crohns and I did, so keep asking questions, search on internet, etc...Stay strong!
 

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